Catalog Number
06K3851
Brand Name
ARCHITECT
Version/Model Number
06K3851
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
Yes
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
GTQ
Product Code Name
ANTISTREPTOLYSIN - TITER/STREPTOLYSIN O REAGENT
Public Device Record Key
91d8d3f3-da80-4aac-80d8-c5469769665e
Public Version Date
March 11, 2020
Public Version Number
1
DI Record Publish Date
March 03, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 259 |
2 | A medical device with a moderate to high risk that requires special controls. | 245 |
U | Unclassified | 5 |